N. Mahlaoui, V. Minard-colin, C. Picard, A. Bolze, C. Ku et al., Isolated Congenital Asplenia: A French Nationwide Retrospective Survey of 20 Cases, The Journal of Pediatrics, vol.158, issue.1, pp.142-148, 2011.
DOI : 10.1016/j.jpeds.2010.07.027

A. Bolze, N. Mahlaoui, M. Byun, B. Turner, N. Trede et al., Ribosomal Protein SA Haploinsufficiency in Humans with Isolated Congenital Asplenia, Science, vol.340, issue.6135, pp.976-978
DOI : 10.1126/science.1234864

L. Garavelli and P. Mainardi, Mowat-Wilson syndrome, Orphanet Journal of Rare Diseases, vol.2, issue.1, p.42, 2007.
DOI : 10.1186/1750-1172-2-42

D. Mowat, G. Croaker, D. Cass, B. Kerr, J. Chaitow et al., Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23., Journal of Medical Genetics, vol.35, issue.8, pp.35617-623, 1998.
DOI : 10.1136/jmg.35.8.617

L. Garavelli, A. Donadio, C. Zanacca, G. Banchini, D. Giustina et al., Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome, Am J Med Genet Part A, vol.116, issue.4, pp.385-388, 2003.

G. Verstappen, L. Van-grunsven, C. Michiels, T. Van-de-putte, J. Souopgui et al., Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex, Human Molecular Genetics, vol.17, issue.8, pp.171175-1183, 2008.
DOI : 10.1093/hmg/ddn007

C. Zweier, C. Thiel, A. Dufke, Y. Crow, P. Meinecke et al., Clinical and Mutational Spectrum of Mowat???Wilson Syndrome, European Journal of Medical Genetics, vol.48, issue.2, pp.97-111, 2005.
DOI : 10.1016/j.ejmg.2005.01.003

G. Bassez, O. Camand, V. Cacheux, A. Kobetz, F. Dastot-le-moal et al., Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the ???Mowat???Wilson??? syndrome, Neurobiology of Disease, vol.15, issue.2, pp.240-250, 2004.
DOI : 10.1016/j.nbd.2003.10.004

D. Mowat, M. Wilson, and M. Goossens, Mowat-Wilson syndrome, Journal of Medical Genetics, vol.40, issue.5, pp.305-310, 2003.
DOI : 10.1136/jmg.40.5.305

M. Rosado, F. Gesualdo, V. Marcellini, D. Sabatino, A. Corazza et al., Preserved antibody levels and loss of memory B cells against pneumococcus and tetanus after splenectomy: Tailoring better vaccination strategies, European Journal of Immunology, vol.111, issue.10, pp.432659-2670
DOI : 10.1002/eji.201343577

D. Moal, F. Wilson, M. Mowat, D. Collot, N. Niel et al., ZFHX1B mutations in patients with Mowat-Wilson syndrome, Human Mutation, vol.140, issue.4, pp.313-321, 2007.
DOI : 10.1002/humu.20452